Washington Healthcare Update
Jul 31, 2023
Charles Kelley
14 mins
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This Week in Washington: Senate Finance Committee reports out Modernizing and Ensuring PBM Accountability Act; House Ways and Means Committee reports out healthcare bills; Senate Appropriations Committee reports out FY 2024 Labor-HHS funding bill; Congress leaves for August recess
Congress
House
- House Ways and Means Committee Marks Up Two Healthcare Bills
- House Energy and Commerce Committee Chairman Issues Drug Shortage Discussion Draft
Senate
- Senate Finance Committee Marks Up Modernizing and Ensuring PBM Accountability Act
- Senate Appropriations Committee Marks Up FY 2024 Labor-HHS Funding Bill
- Senate HELP Committee Chairman Cancels Two Days of Mark Ups
Administration
- CMS Releases Medicaid and CHIP Coverage Renewal Data
- CMS Releases Medicaid and CHIP Mental Health and SUD Action Plan Overview and Guide
- CMS Updates Overall Hospital Quality Star Ratings
- CMS Issues Civil Monetary Penalties Over Hospital Price Transparency Non-Compliance
- FDA Approves Second OTC Naloxone Nasal Spray
- FDA Releases Draft Guidance on Opioid Use Disorder Device Innovation
- FDA Approves Warfarin Therapy Reversal Drug
- FDA Approves Pediatric Pulmonary Artery Stenosis Stent
- FDA Approves Anthrax Post-Exposure Vaccine
- HRSA Awards $11 Million Toward Healthcare Workforce Residency Programs
Proposed Rules
- CMS Proposed Rule Strengthens Coverage of Mental Health Insurance Benefits
- CMS Proposed Rule Contains RFI on Episode-based Payment Model
- CMS Proposed Rule Updates CY 2024 Medicare PFS Payments
- CMS Proposed Rule Revises FY 2024 Medicare Hospital OPPS and ASC Payment Systems
- CMS Proposed Rule Updates Medicare Home Health PPS Rates for CY 2024
- CMS Proposed Rule Outlines Remedy to 340B Program Payment Adjustments
- CMS Proposed Rule Modifies Definition of Short-term Health Plans
- CMS Proposed Rule Updates and Revises ESRD PPS for CY 2024
- FDA Proposes Rule to Broaden Prescription Drug Labeling Regulations
- FDA Proposes New Tobacco Product Manufacturing Practices Requirements
- OCR Proposed Rule Reaffirms Federal Discrimination Protections in HHS Grants
Final Rules
- CMS Final Rule Updates Hospice Wage Index and Payment Rate in FY 2024
- CMS Final Rule Updates PPS Rates for Inpatient Psychiatric Facilities in FY 2024
- CMS Final Rule Updates PPS Rates for Inpatient Rehabilitation Facilities in FY 2024
- OIG Final Rule Outlines Civil Money Penalty Regulations
- CMS Final Rule Clarifies Medicare DSH Payment Adjustment Part C Days
- CMS Final Rule Eliminates COVID-19 Healthcare Worker Vaccination Requirement
- DEA Releases Temporary Rule Extending COVID-19 Telemedicine Flexibilities
- CMS Finalizes 2024 Medicare Advantage and Part C and D Payment Policies
- FDA Issues Final Rule Regarding Mammography Quality Standards
- FDA Delays Tobacco Product Required Warning Final Rule Effective Date
Reports
CBO Cost Estimates
- CBO Responds to Request for Cost Estimate on Primary Care and Health Workforce Expansion Act
- CBO Releases Preliminary Cost Estimate of the Modernizing and Ensuring PBM Accountability Act
Other
Upcoming Hearings
House The House has recessed for its August district work period. Senate The Senate has recessed for its August state work period.Congress
House
House Ways and Means Committee Marks Up Two Healthcare Bills On July 26, the House Ways and Means Committee reported out two healthcare bills on a party line vote. The bills are: H.R. 4822, the Health Care Price Transparency Act of 2023 This legislation would implement additional site-neutral payment cuts and regulatory measures on off-campus hospital outpatient departments. It would also impose Medicare sequester cuts on hospitals, codify hospital price transparency regulations, require healthcare plans to limit beneficiary cost-sharing for a month’s supply of a drug covered under Medicare Part D, and establish an electronic prior authorization system for Medicare Advantage plans. H.R. 3284, the Providers and Payers COMPETE Act This legislation would require the Secretary of Health and Human Services (HHS) to submit an annual report to Congress outlining the effects of Medicare payment rules on provider and payer consolidation. The report would also detail the effects of payer and provider consolidation with respect to Centers for Medicare and Medicaid (CMS) Innovation Center models. During the markup, the committee rejected four amendments. Among them was an amendment offered by Rep. Pascrell (D-NJ) that would have required the disclosure of hospitals and nursing homes owned by private equity entities. For more information, click here. House Energy and Commerce Committee Chairman Issues Drug Shortage Discussion Draft On July 28, House Energy and Commerce Committee Chairman Cathy McMorris Rodgers (R-WA) released a discussion draft concerning drug shortages. The discussion draft outlines proposals that the committee developed from stakeholder feedback from a request for information (RFI) the Chair and Senate Finance Committee Ranking Member Mike Crapo (R-ID) issued on drug shortages in June. Among the policy proposals are provisions that would:- Exempt certain specified drugs from increases in rebates under the Medicaid program;
- Implement a cap on total rebates for certain generic drugs;
- Exempt generic, sterile injection drugs from the 340B Drug Discount Program;
- Direct the Government Accountability Office (GAO) to study the number of generic drugs that are subject to 340B penny pricing;
- Direct the Health Resources and Services Administration (HRSA) to issue guidance on preventing drug diversions during shortages;
- Reduce inflation rebate amounts for certain shortage drugs subject to rebate waivers under the Medicare program;
- Direct the Department of Health and Human Services (HHS) to study Medicare coding policies for generic sterile injectables and other Part B drugs facing shortages;
- Strengthen reporting requirements for Group Purchasing Organizations; and
- Require the Food and Drug Administration (FDA) to issue noncompliance letters relating to drug volume reporting.
Senate
Senate Finance Committee Marks Up Modernizing and Ensuring PBM Accountability Act On July 26, on a 26 to 1 vote, the Senate Finance Committee reported out of committee the Modernizing and Ensuring PBM Accountability (MEPA) Act. The legislation would update federal prescription drug programs and implement provisions aimed at reforming pharmacy benefit manager (PBM) practices. It would:- Prohibit PBMs and their affiliates from deriving income or renumeration for Medicare Part D covered drugs based on a manufacturer’s price for the drug;
- Require PBMs to define and apply drug and drug pricing terms in contracts with Part D plan sponsors in a transparent and consistent manner;
- Strengthen PBM reporting requirements and expand the amount of information that PBMs provide to Part D plan sponsors and the Secretary of Health and Human Services (HHS);
- Allow Part D plan sponsors to audit their PBM for compliance with contract requirements;
- Require the HHS Secretary to implement standard Part D measures to assess network pharmacy performance;
- Ban PBM spread pricing in the Medicaid program; and
- Require retail community pharmacies to participate in the National Average Drug Acquisition Cost (NADAC) survey.
- Authorize $47.8 billion in funding for the National Institutes of Health (NIH);
- Authorize $5 billion in funding for opioid and substance use disorder treatment and prevention programs;
- Authorize $1.5 billion in funding for the NIH Advanced Research Projects Agency for Health (ARPA-H);
- Authorize $3.67 billion in funding for the Administration for Strategic Preparedness and Response (ASPR);
- Retain funding for the Teen Pregnancy Prevention Program;
- Increase funding for the Ending the HIV Epidemic Initiative;
- Increase funding for childcare and mental health programs; and
- Award $2 billion in additional emergency funding to HHS.
Administration
CMS Releases Medicaid and CHIP Coverage Renewal Data On July 28, the Centers for Medicare and Medicaid Services (CMS) released data on ongoing Medicaid and Children’s Health Insurance Program (CHIP) coverage renewals. The data revealed that 715,000 people lost their Medicaid coverage in April and 500,000 renewals remain pending. Approximately 80 percent of disenrollments have occurred due to procedural reasons, and nearly half of renewals were conducted on an ex parte basis. For more information, click here. CMS Releases Medicaid and CHIP Mental Health and SUD Action Plan Overview and Guide On July 25, the Centers for Medicare and Medicaid Services (CMS) released the Medicaid and Children’s Health Insurance Program (CHIP) Mental Health (MH) and Substance Use Disorder (SUD) Action Plan overview and guide. The overview and guide outline the strategies CMS is using to improve treatment and support of enrollees with these conditions. CMS is primarily focused on increasing access to prevention and treatment services, expanding home- and community-based services and coverage of non-traditional services and settings, and improving the quality of care for MH and SUD conditions. For more information on the action plan overview, click here. For more information on the action plan guide, click here. CMS Updates Overall Hospital Quality Star Ratings On July 26, the Centers for Medicare and Medicaid Services (CMS) updated the overall hospital quality star ratings on the CMS Care Compare website. The Care Compare website allows patients and caregivers to compare hospitals and access information on more than 100 quality measures. For the first time, CMS has included Veterans Health Administration (VA) hospitals in its annual quality star ratings update. For more information, click here. CMS Issues Civil Monetary Penalties Over Hospital Price Transparency Non-Compliance On July 25, the Centers for Medicare and Medicaid Services (CMS) announced that it had imposed civil monetary penalties on three hospitals that were not complying with the Hospital Price Transparency Final Rule that went into effect on Jan. 1, 2021. The final rule requires all hospitals to disclose the standard charges for items and services they provide. For more information, click here. FDA Approves Second OTC Naloxone Nasal Spray On July 28, the Food and Drug Administration (FDA) approved RiVive, an over-the-counter (OTC) naloxone hydrochloride nasal spray intended to reverse a known or suspected opioid overdose. This is the second OTC naloxone nasal spray to be granted FDA approval. The FDA decided to grant RiVive approval after data showed that it was as effective as an approved prescription naloxone product. For more information, click here. FDA Releases Draft Guidance on Opioid Use Disorder Device Innovation On July 27, the Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) released draft guidance outlining how clinical studies for devices seeking to treat opioid use disorder (OUD) should be designed to support marketing submissions. The draft guidance recommends that stakeholders control for bias, monitor drug use, conduct follow-up studies and evaluate participant retention and data analysis plans. The FDA is seeking comments on the draft guidance and will accept them until Oct. 26. For more information, click here. FDA Approves Warfarin Therapy Reversal Drug On July 21, the Food and Drug Administration (FDA) approved Balfaxar (prothrombin complex concentrate, human-lans), a drug intended to rapidly restore the blood coagulation factor in adult patients undergoing vitamin K antagonist and warfarin therapy before an urgent surgical or invasive procedure. Patients undergoing warfarin therapy are at significant risk of experiencing heavy bleeding during invasive procedures. Balfaxar seeks to reduce this risk by replenishing the levels of blood clotting factors in patients. The FDA decided to grant the drug approval after a randomized, double-blind, multicenter study showed that the drug had a similar efficacy rate as its comparator drug Kcentra. For more information, click here. FDA Approves Pediatric Pulmonary Artery Stenosis Stent On July 21, the Food and Drug Administration (FDA) approved the Cordis Palmaz Mullins XD Pulmonary Stent. The stent is intended to treat pediatric patients who are receiving treatment for pulmonary artery stenosis (PAS), a heart condition in which the pulmonary artery narrows and prevents normal blood flow. For more information, click here. FDA Approves Anthrax Post-Exposure Vaccine On July 20, the Food and Drug Administration (FDA) approved Cyfendus (anthrax vaccine adsorbed, adjuvanted), a vaccine intended to be administered to patients 18 to 65 years old following suspected or confirmed exposure to Bacillus anthracis. The FDA is recommending that the vaccine be administered in conjunction with other recommended antibacterial drugs. For more information, click here. HRSA Awards $11 Million Toward Healthcare Workforce Residency Programs On July 26, the Health Resources and Services Administration (HRSA) announced that it had awarded $11 million toward programs focused on implementing medical residency programs in rural communities. The funding is intended to help address the shortage of medical health professionals and lack of access to care in rural areas. For more information, click here.Proposed Rules
CMS Proposed Rule Strengthens Coverage of Mental Health Insurance Benefits On July 25, the Centers for Medicare and Medicaid Services (CMS) released a proposed rule that would implement amendments relating to the Paul Wellstone and Pete Domenici Mental Health Parity and Addiction Equity Act of 2008 (MHPAEA). The proposed rule would:- Clarify that the MHPAEA ensures an individual’s right to access mental health and substance use disorder benefits in parity with medical/surgical benefits;
- Provide examples that make clear that plans and issuers may not use restrictive prior authorization and other medical management techniques or standards related to network composition for mental health and substance use disorder benefits;
- Clarify that certain factors may not be used to determine out-of-network reimbursement rates for mental health and substance use disorder providers;
- Require plans and issuers to gather and analyze outcomes data and take action to resolve material differences in access to mental health and substance use disorder benefits and medical/surgical benefits;
- Codify a requirement that directs plans and issuers to conduct meaningful comparative analyses to measure the impact of nonquantitative treatment limitation (NQTL); and
- Implement a sunset provision adopted in the Consolidated Appropriations Act of 2023, that allows self-funded, non-federal government plan elections to opt out of compliance with MHPAEA.
- Decrease the conversion factor by 3.34 percent to $32.75;
- Delay implementation of a policy that defines the substantive portion of a split or shared visit based on the amount of time spent by a billing practitioner;
- Create a new benefit category for marriage and family therapists and mental health counselors under Medicare Part B;
- Establish new payment codes for mobile psychotherapy for crisis services;
- Implement five new optional Merit-based Incentive Payment System Value Reporting Pathways; and
- Extend several telehealth waivers.
- Increase OPPS payment rates for hospitals that meet applicable quality reporting requirements by 2.8 percent. This is based off of a projected hospital market basket percentage increase of 3.0 percent minus a 0.2 percent productivity adjustment;
- Update the productivity-adjusted hospital market basket update factor to ASC rates by 2.8 percent and extend its application through calendar years (CYs) 2024 and 2025;
- Establish the Intensive Outpatient Program (IOP) under Medicare and implement various IOP service provisions;
- Update partial hospitalization program (PHP) Medicare payment rates;
- Strengthen hospital price transparency;
- Adopt and codify several standard quality program reporting policies; and
- Expand access to behavioral healthcare and promote safe and effective patient-centered care.
- Apply a permanent PPS adjustment of negative 5.653 percent;
- Cut reimbursement rates for home health providers by 2.2 percent;
- Add and remove quality measures from the Home Health quality reporting program;
- Codify requirements for negative wound therapy;
- Establish regulations and implement the items and services payment for lymphedema compression treatment and home intravenous globulin services;
- Address concerns about unnecessary utilization, costs and care quality; and
- Add an informal dispute resolution (IDR) and special focus program (SFP) for hospice
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